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Gene: ELK1 |
Gene summary for ELK1 |
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Gene information | Species | Human | Gene symbol | ELK1 | Gene ID | 2002 |
Gene name | ETS transcription factor ELK1 | |
Gene Alias | ELK1 | |
Cytomap | Xp11.23 | |
Gene Type | protein-coding | GO ID | GO:0001889 | UniProtAcc | A0A024R1A7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
2002 | ELK1 | LZE4T | Human | Esophagus | ESCC | 9.23e-05 | 6.38e-02 | 0.0811 |
2002 | ELK1 | LZE7T | Human | Esophagus | ESCC | 2.42e-02 | 1.30e-01 | 0.0667 |
2002 | ELK1 | LZE8T | Human | Esophagus | ESCC | 3.95e-04 | 9.27e-02 | 0.067 |
2002 | ELK1 | LZE24T | Human | Esophagus | ESCC | 5.58e-16 | 1.79e-01 | 0.0596 |
2002 | ELK1 | P2T-E | Human | Esophagus | ESCC | 1.60e-12 | 3.32e-01 | 0.1177 |
2002 | ELK1 | P4T-E | Human | Esophagus | ESCC | 1.55e-11 | 2.62e-01 | 0.1323 |
2002 | ELK1 | P5T-E | Human | Esophagus | ESCC | 7.96e-07 | 5.63e-02 | 0.1327 |
2002 | ELK1 | P8T-E | Human | Esophagus | ESCC | 7.51e-12 | 2.46e-01 | 0.0889 |
2002 | ELK1 | P9T-E | Human | Esophagus | ESCC | 5.71e-06 | 6.35e-02 | 0.1131 |
2002 | ELK1 | P10T-E | Human | Esophagus | ESCC | 1.14e-09 | 1.81e-01 | 0.116 |
2002 | ELK1 | P11T-E | Human | Esophagus | ESCC | 8.78e-07 | 3.72e-01 | 0.1426 |
2002 | ELK1 | P12T-E | Human | Esophagus | ESCC | 2.69e-13 | 1.21e-01 | 0.1122 |
2002 | ELK1 | P15T-E | Human | Esophagus | ESCC | 4.72e-09 | 2.02e-01 | 0.1149 |
2002 | ELK1 | P16T-E | Human | Esophagus | ESCC | 2.96e-23 | 4.76e-01 | 0.1153 |
2002 | ELK1 | P17T-E | Human | Esophagus | ESCC | 3.28e-05 | 1.35e-01 | 0.1278 |
2002 | ELK1 | P20T-E | Human | Esophagus | ESCC | 9.68e-14 | 3.89e-01 | 0.1124 |
2002 | ELK1 | P21T-E | Human | Esophagus | ESCC | 3.72e-20 | 3.09e-01 | 0.1617 |
2002 | ELK1 | P22T-E | Human | Esophagus | ESCC | 3.75e-20 | 3.99e-01 | 0.1236 |
2002 | ELK1 | P23T-E | Human | Esophagus | ESCC | 1.84e-15 | 4.24e-01 | 0.108 |
2002 | ELK1 | P24T-E | Human | Esophagus | ESCC | 1.92e-05 | 1.14e-01 | 0.1287 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:001021217 | Esophagus | ESCC | response to ionizing radiation | 110/8552 | 148/18723 | 1.11e-12 | 4.78e-11 | 110 |
GO:0048732111 | Esophagus | ESCC | gland development | 269/8552 | 436/18723 | 7.81e-12 | 2.95e-10 | 269 |
GO:000931419 | Esophagus | ESCC | response to radiation | 277/8552 | 456/18723 | 4.42e-11 | 1.43e-09 | 277 |
GO:007121419 | Esophagus | ESCC | cellular response to abiotic stimulus | 206/8552 | 331/18723 | 7.52e-10 | 1.88e-08 | 206 |
GO:010400419 | Esophagus | ESCC | cellular response to environmental stimulus | 206/8552 | 331/18723 | 7.52e-10 | 1.88e-08 | 206 |
GO:007147816 | Esophagus | ESCC | cellular response to radiation | 122/8552 | 186/18723 | 3.07e-08 | 5.73e-07 | 122 |
GO:0070997111 | Esophagus | ESCC | neuron death | 216/8552 | 361/18723 | 3.49e-08 | 6.45e-07 | 216 |
GO:0071479110 | Esophagus | ESCC | cellular response to ionizing radiation | 54/8552 | 72/18723 | 3.85e-07 | 5.32e-06 | 54 |
GO:0061008110 | Esophagus | ESCC | hepaticobiliary system development | 98/8552 | 150/18723 | 8.91e-07 | 1.15e-05 | 98 |
GO:0001889110 | Esophagus | ESCC | liver development | 96/8552 | 147/18723 | 1.18e-06 | 1.47e-05 | 96 |
GO:1901214111 | Esophagus | ESCC | regulation of neuron death | 186/8552 | 319/18723 | 3.35e-06 | 3.73e-05 | 186 |
GO:00303239 | Esophagus | ESCC | respiratory tube development | 112/8552 | 181/18723 | 7.82e-06 | 7.69e-05 | 112 |
GO:00605417 | Esophagus | ESCC | respiratory system development | 123/8552 | 203/18723 | 1.26e-05 | 1.15e-04 | 123 |
GO:00303249 | Esophagus | ESCC | lung development | 109/8552 | 177/18723 | 1.40e-05 | 1.27e-04 | 109 |
GO:1901654111 | Esophagus | ESCC | response to ketone | 118/8552 | 194/18723 | 1.45e-05 | 1.31e-04 | 118 |
GO:1901216111 | Esophagus | ESCC | positive regulation of neuron death | 65/8552 | 97/18723 | 1.76e-05 | 1.56e-04 | 65 |
GO:000941611 | Esophagus | ESCC | response to light stimulus | 183/8552 | 320/18723 | 2.03e-05 | 1.76e-04 | 183 |
GO:001033215 | Esophagus | ESCC | response to gamma radiation | 41/8552 | 56/18723 | 2.64e-05 | 2.21e-04 | 41 |
GO:007148010 | Esophagus | ESCC | cellular response to gamma radiation | 23/8552 | 31/18723 | 1.20e-03 | 5.88e-03 | 23 |
GO:19016556 | Esophagus | ESCC | cellular response to ketone | 59/8552 | 96/18723 | 1.32e-03 | 6.30e-03 | 59 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa05166211 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa0520529 | Esophagus | ESCC | Proteoglycans in cancer | 138/4205 | 205/8465 | 1.79e-07 | 1.40e-06 | 7.15e-07 | 138 |
hsa05163210 | Esophagus | ESCC | Human cytomegalovirus infection | 148/4205 | 225/8465 | 5.73e-07 | 4.00e-06 | 2.05e-06 | 148 |
hsa051619 | Esophagus | ESCC | Hepatitis B | 108/4205 | 162/8465 | 7.68e-06 | 4.15e-05 | 2.12e-05 | 108 |
hsa0521320 | Esophagus | ESCC | Endometrial cancer | 45/4205 | 58/8465 | 1.14e-05 | 5.98e-05 | 3.06e-05 | 45 |
hsa0522518 | Esophagus | ESCC | Hepatocellular carcinoma | 109/4205 | 168/8465 | 4.27e-05 | 1.88e-04 | 9.64e-05 | 109 |
hsa0451020 | Esophagus | ESCC | Focal adhesion | 127/4205 | 203/8465 | 1.25e-04 | 4.99e-04 | 2.56e-04 | 127 |
hsa049109 | Esophagus | ESCC | Insulin signaling pathway | 89/4205 | 137/8465 | 1.97e-04 | 7.32e-04 | 3.75e-04 | 89 |
hsa0401218 | Esophagus | ESCC | ErbB signaling pathway | 56/4205 | 85/8465 | 1.78e-03 | 5.24e-03 | 2.68e-03 | 56 |
hsa05166310 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa0520537 | Esophagus | ESCC | Proteoglycans in cancer | 138/4205 | 205/8465 | 1.79e-07 | 1.40e-06 | 7.15e-07 | 138 |
hsa0516338 | Esophagus | ESCC | Human cytomegalovirus infection | 148/4205 | 225/8465 | 5.73e-07 | 4.00e-06 | 2.05e-06 | 148 |
hsa0516114 | Esophagus | ESCC | Hepatitis B | 108/4205 | 162/8465 | 7.68e-06 | 4.15e-05 | 2.12e-05 | 108 |
hsa05213110 | Esophagus | ESCC | Endometrial cancer | 45/4205 | 58/8465 | 1.14e-05 | 5.98e-05 | 3.06e-05 | 45 |
hsa0522519 | Esophagus | ESCC | Hepatocellular carcinoma | 109/4205 | 168/8465 | 4.27e-05 | 1.88e-04 | 9.64e-05 | 109 |
hsa04510111 | Esophagus | ESCC | Focal adhesion | 127/4205 | 203/8465 | 1.25e-04 | 4.99e-04 | 2.56e-04 | 127 |
hsa0491014 | Esophagus | ESCC | Insulin signaling pathway | 89/4205 | 137/8465 | 1.97e-04 | 7.32e-04 | 3.75e-04 | 89 |
hsa0401219 | Esophagus | ESCC | ErbB signaling pathway | 56/4205 | 85/8465 | 1.78e-03 | 5.24e-03 | 2.68e-03 | 56 |
hsa0491041 | Liver | HCC | Insulin signaling pathway | 95/4020 | 137/8465 | 1.53e-07 | 1.97e-06 | 1.10e-06 | 95 |
hsa0516622 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
ELK1 | SNV | Missense_Mutation | novel | c.923N>G | p.Ser308Cys | p.S308C | P19419 | protein_coding | deleterious(0.02) | benign(0.054) | TCGA-A7-A26J-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD |
ELK1 | SNV | Missense_Mutation | c.145N>T | p.Arg49Cys | p.R49C | P19419 | protein_coding | deleterious(0) | benign(0.2) | TCGA-BH-A0H9-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
ELK1 | SNV | Missense_Mutation | rs753575056 | c.581N>T | p.Ser194Leu | p.S194L | P19419 | protein_coding | tolerated(0.22) | benign(0) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ELK1 | SNV | Missense_Mutation | novel | c.1280N>G | p.Lys427Arg | p.K427R | P19419 | protein_coding | deleterious(0.01) | benign(0.283) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD |
ELK1 | SNV | Missense_Mutation | c.260N>G | p.Ser87Cys | p.S87C | P19419 | protein_coding | tolerated(0.07) | benign(0.362) | TCGA-E2-A14W-01 | Breast | breast invasive carcinoma | Male | >=65 | I/II | Chemotherapy | cytoxan | SD | |
ELK1 | insertion | Frame_Shift_Ins | novel | c.1138_1139insCAGACTGGGTGACCAAAACCACATGTGAGAGACTACGTGGGCAT | p.Ser380ThrfsTer18 | p.S380Tfs*18 | P19419 | protein_coding | TCGA-AN-A04A-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | ||
ELK1 | SNV | Missense_Mutation | novel | c.1052N>T | p.Ala351Val | p.A351V | P19419 | protein_coding | deleterious(0.03) | possibly_damaging(0.493) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ELK1 | SNV | Missense_Mutation | novel | c.902N>T | p.Ala301Val | p.A301V | P19419 | protein_coding | tolerated(0.35) | benign(0.054) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ELK1 | SNV | Missense_Mutation | novel | c.172N>A | p.Asp58Asn | p.D58N | P19419 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ELK1 | SNV | Missense_Mutation | c.1226N>T | p.Ser409Phe | p.S409F | P19419 | protein_coding | tolerated(0.13) | possibly_damaging(0.804) | TCGA-C5-A1BQ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | CR |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
2002 | ELK1 | TRANSCRIPTION FACTOR | DHPG | 12220559 |
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